Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113513108-113513235 | Common:2; Rare:20 | ||||
chr1:113693821-113694053 | Common:1; Rare:38 | ||||
chr1:116376569-116376671 | Rare:15 | ||||
chr1:116384576-116384853 | Rare:78 | ||||
chr1:116392561-116392872 | Common:2; Rare:62 | ||||
chr1:116394928-116395295 | Common:3; Rare:74 | ||||
chr1:116396489-116396670 | Rare:34 | ||||
chr1:117928823-117929001 | Rare:46 | ||||
chr1:119743792-119743973 | Common:1; Rare:48; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:119755153-119755428 | Common:2; Rare:66; Clinvar (pathogenic):1 | ||||
chr1:120341948-120342066 | Common:1; Rare:23 | ||||
chr1:120342159-120342462 | Rare:63 | ||||
chr1:120463109-120463124 | Rare:5 | ||||
chr1:120464225-120464394 | Rare:23 | ||||
chr1:120464456-120464468 | Rare:2 |